Methods of generating and using antibody-producing cells

ABSTRACT

An objective of the present invention is to facilitate the acquisition of antibody-producing cells that are infiltrating virus-infected cells, cancer cells, abnormal cells forming a benign hyperplasia, and the like, and to improve the efficiency of the production of antibodies as well as nucleic acids encoding them from the antibody-producing cells. 
     The present inventors discovered that, when cancer tissues comprising infiltrating lymphocytes are transplanted into highly immunodeficient animals that do not have T cells, B cells, and NK cells and further exhibit a low IFN production ability, the differentiation and proliferation of infiltrating lymphocytes are unexpectedly promoted, and the number of plasma cells that produce antibodies recognizing cancer tissues increases dramatically, plasma cells can be separated easily, and antibodies or nucleic acids encoding them can be easily prepared from the plasma cells.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 11/587,701 (now U.S. Pat. No. 8,008,076), having a 371(c) date of Nov. 8, 2007, which is the National Stage of International Application No. PCT/JP2005/007962, filed on Apr. 27, 2005, which claims the benefit of Japanese Patent Application No. 2004-132019, filed on Apr. 27, 2004. The contents of each of the foregoing applications are hereby incorporated by reference in their entireties.

TECHNICAL FIELD

The present invention relates to the acquisition of antibody-producing cells. Moreover, the present invention relates to methods for producing antibodies and antibody-encoding nucleic acids from these antibody-producing cells.

BACKGROUND ART

The infiltration of lymphocytes into cancer and lesion tissues is a phenomenon which has been clinically known for a long time (Non-Patent Documents 1, 2, 3, 4, and 5). Moreover, numerous experimental and clinical data indicate that infiltrated lymphocytes attack cancer and lesion tissues (Non-Patent Documents 6, 7, and 8).

The main players of cellular immunity in cancer are cytotoxic T cells (CTL) and NK cells (Non-Patent Documents 9, 10, 11, and 12), while the main players of humoral immunity are antibodies produced by plasma cells (Non-Patent Documents 13, 14, and 15). Antibodies that recognize cancer antigens have been shown to be present in the serum of cancer patients and novel cancer antigens have been isolated using antibodies from cancer patients (Non-Patent Documents 16 and 17). Moreover, some of the antibodies produced by plasma cells that infiltrate cancer tissues have been demonstrated to bind to cancer cells (Non-Patent Documents 18, 19, and 20). In addition, antibodies such as Herceptin and Rituxan, which recognize antigens strongly expressed in cancers, have been developed as therapeutic drugs, demonstrating the utility of antibodies that recognize cancer-specific antigens (Non-Patent Documents 21 and 22).

Although attempts have been made to separate plasma cells that infiltrate cancer tissues and to continuously produce specific antibodies from those cells, these attempts have failed so far. Reasons for the failure include the inability to secure tumor-specific plasma cells (B lymphocytes) in sufficient numbers because of the difficulty of separating them from cancer tissues, and even if separation were successful to some extent, the instability of antibody production with methods that use EBV or hybridomas for immortalizing antibody-producing cells.

On the other hand, recombinant DNA technologies for creating antibodies having antigen-binding activities similar to those from cloned antibody-producing cells, namely methods for cloning antibody genes and preparing recombinant antibody proteins, are being established (Non-Patent Documents 23 and 24). Antibody genes such as Fv, scFv, Fab, IgG, or IgM (Non-Patent Documents 25, 26, and 27) can be produced by cloning genes encoding the variable regions of antibody genes. scFv, which is the smallest recombinant antibody molecule, has a structure in which a heavy chain variable region and a light chain variable region are joined by a linker.

Cloned B cells express a single antibody gene. Thus, it is easy to clone heavy chain and light chain variable regions from these cells. However, since B cells present in peripheral blood and B cells that infiltrate cancer tissues are cell groups (polyclones) producing various antibodies (Non-Patent Documents 28 and 29), it is extremely difficult to clone cancer-specific genes from these.

-   [Non-Patent Document 1] Hurliamnn et al. (1985) Int J Cancer 35:753. -   [Non-Patent Document 2] Whiteside et al. (1986) Cancer Immunol     Immunother 23:169, -   [Non-Patent Document 3] Wolf et al. (1986) Otolaryngol Head Neck     Surg 95:142. -   [Non-Patent Document 4] Husby et al (1976) J Clin Invest 57:1471, -   [Non-Patent Document 5] Vose et al. (1979) Int J Cancer 24:579. -   [Non-Patent Document 6] Rosenberg et al. (1988) New England J Med     319:1676. -   [Non-Patent Document 7] Van Pel et al, (1995) Immunol Reviews     145:229. -   [Non-Patent Document 8] Kreider et al. (1984) Cancer Metastasis Rev     3:53. -   [Non-Patent Document 9] Nobholz and MacDonald (1983) Annu Rev     Immunol 1:273. -   [Non-Patent Document 10] Gerundolo et al. (1987) Eur J Immunol     17:173. -   [Non-Patent Document 11] Hanna et al. (1984) Cancer Inv Met 309. -   [Non-Patent Document 12] Brittenden et al. (1996) Cancer 77:1226. -   [Non-Patent Document 13] Roitt et al. (1969) Lancet 2:367. -   [Non-Patent Document 14] Borsos (1971) Progress in Immunology: p841.     New York, Academic Press. -   [Non-Patent Document 15] Kodera and Bean (1975) Int J Cancer 16:579. -   [Non-Patent Document 16] Yao-Tseng Chen et al. (1997) Proc Natl Acad     Sci USA 94:1914. -   [Non-Patent Document 17] Ugur Sahin et al. (1997) Cancer 9:709, -   [Non-Patent Document 18] Williams et al. (1996) Jour Immunol     156:1908. -   [Non-Patent Document 19] Imahayashi et al. (2000) Cancer Invest     18:530. -   [Non-Patent Document 20] Yasuda et al. (2002) Cancer Res 62:1751. -   [Non-Patent Document 21] Green et al. (2000) Cancer Treat Rev     26:269. -   [Non-Patent Document 22] Maloney et al. (1997) Blood 90:2188. -   [Non-Patent Document 23] Marks et al. (1991) J Mol Biol 222:581. -   [Non-Patent Document 24] Larrick et al. (1992) Immunol reviews     130:69. -   [Non-Patent Document 25] Skerra et al. (1988) Science 240:293. -   [Non-Patent Document 26] Bird et al, (1988) Science 242:243. -   [Non-Patent Document 27] Better et al. (1988) Science 240:104. -   [Non-Patent Document 28] Kotlan et al. (1999) Immunol Lett 65:143. -   [Non-Patent Document 29] Hansen et al. (2001) Pro Natl Acad Sci USA     98:12659. -   [Non-Patent Document 30] Blood, 100: 3175-3182, 2002.

DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention

An objective of the present invention is to facilitate the acquisition of antibody-producing cells infiltrating lesion tissues framed by abnormal cells (such as virus-infected cells, cancer cells, and abnormal cells forming benign hyperplasia). An objective of the present invention is to provide methods for producing antibodies from antibody-producing cells infiltrating lesion tissues, and nucleic acids encoding these antibodies. In addition, the present invention provides antibodies produced based on antibody-producing cells infiltrating lesion tissues, and nucleic acids encoding these antibodies. Moreover, an objective of the present invention is to provide therapeutic or diagnostic compositions against lesion tissues using antibody-producing cells infiltrating lesion tissues, antibodies obtained based on these cells, and nucleic acids encoding these antibodies.

Means to Solve the Problems

In view of the aforementioned problems, the present inventors conducted dedicated research to discover that, when cancer tissues comprising infiltrating lymphocytes are transplanted into the highly immunodeficient NOD/SCID/γ_(c) ^(null) mice (Non-Patent Document 30, referred to as “NOG mice” in the present application) which do not have any T cells, B cells, or NK cells and which exhibit a low IFN production ability, the differentiation and proliferation of infiltrating lymphocytes are unexpectedly promoted, the number of plasma cells producing antibodies that recognize cancer tissues are dramatically increased, and that these cells can be easily separated. These findings led to the completion of the present invention. Specifically, the present invention is as described below:

(1) a method of proliferating plasma cells, wherein the method comprises the step of transplanting a tissue comprising plasma cells, blood comprising plasma cells, or plasma cells collected from a tissue or blood, into a highly immunodeficient non-human animal; (2) the method of proliferation of (1), wherein the tissue is a lesion tissue comprising infiltrating lymphocytes; (3) a method of producing cells which produce an antibody to an abnormal cell comprised in a lesion tissue, wherein the method comprises the steps of:

(a) transplanting a lesion tissue comprising infiltrating lymphocytes into a highly immunodeficient non-human animal;

(b) detecting the proliferation of plasma cells at the site of transplantation; and

(c) recovering a lesion tissue comprising plasma cells from the site of transplantation;

(4) the method of production of (3), further comprising the step of:

(d) excising a plasma cell from the recovered lesion tissue and fusing the plasma cell with a partner cell;

(5) a method of producing a nucleic acid encoding an antibody against an abnormal cell comprised in a lesion tissue, or a portion of the antibody, wherein the method comprises the steps of:

(a) transplanting a lesion tissue comprising infiltrating lymphocytes into a highly immunodeficient non-human animal;

(b) detecting the proliferation of plasma cells at the site of transplantation;

(c) recovering a lesion tissue comprising plasma cells from the site of transplantation; and

(d) obtaining a nucleic acid encoding an antibody from the recovered lesion tissue;

(6) the method of production of (5), wherein step (d) comprises collecting a nucleic acid encoding an antibody from plasma cells after excising the plasma cells from a lesion tissue;

(7) the method of production of (5) or (6) further comprising the step of:

(e) amplifying a nucleic acid encoding an antibody variable region using a nucleic acid encoding an antibody as a template and an oligonucleotide capable of amplifying the antibody variable region;

(8) a method of producing an antibody against an abnormal cell comprised in a lesion tissue, or a portion of the antibody, wherein the antibody is isolated from antibody-producing cells produced according to (3) or (4);

(9) a method of producing an antibody against an abnormal cell comprised in a lesion tissue, or a portion of the antibody, wherein the method comprises the following steps (a) to (c):

(a) introducing into an expression vector a nucleic acid obtained according to the method of production of any one of (5) to (7), or the nucleic acid that has been chimerized or humanized;

(b) transforming a host cell with a vector harboring the nucleic acid; and

(c) producing an antibody by culturing the transformant;

(10) the method of production of (9), further comprising the step of:

(d) contacting the obtained antibody with a lesion tissue and selecting a transformant producing an antibody that binds to the lesion tissue;

(11) the method of any one of (3) to (10), wherein the abnormal cell comprised in the transplanted lesion tissue is a cancer cell, a cell forming a hyperplasia, or a virus-infected cell;

(12) the method of (11), wherein the cancer is a solid cancer or a blood cancer;

(13) the method of (12), wherein the solid cancer is a prostate cancer, stomach cancer, breast cancer, lung cancer, liver cancer, colorectal cancer, or pancreatic cancer;

(14) the method of (11), wherein the hyperplasia is a benign prostatic hyperplasia;

(15) the method of production of any one of (5) to (10), wherein the antibody or a portion thereof is an IgG an IgM, an Fab, an F(ab′)2, an Fv, or a single chain Fv;

(16) the method of production of (9) or (10), wherein the produced antibody or antibody portion is a chimeric antibody, a humanized antibody, a human antibody, or a portion thereof;

(17) a nucleic acid produced according to the method of any one of (5) to (7);

(18) a nucleic acid encoding a chimeric antibody, a humanized antibody, or a human antibody, wherein the nucleic acid comprises the nucleic acid of (17);

(19) an antibody produced according to the method of any one of (8) to (10);

(20) the antibody of (19), which is an antibody against a prostate cancer cell, a stomach cancer cell, a breast cancer cell, a lung cancer cell, a liver cancer cell, a colorectal cancer cell, or a pancreatic cancer cell;

(21) the antibody of (20), which is an antibody against a prostate cancer cell;

(22) the antibody of (21), wherein the antibody recognizes a surface molecule of the prostate cancer cell line DU145;

(23) the antibody of any one of (19) to (22), which is an IgG, an IgM, an Fab, an (Fab′)₂, an Fv, or a single chain Fv;

(24) the antibody of any one of (19) to (22), wherein the antibody comprises a variable region portion;

(25) the antibody of (23) or (24), which is a single chain Fv;

(26) a method of producing a therapeutic composition against a lesion tissue, wherein the method comprises the steps of:

(a) transplanting a lesion tissue infiltrated by lymphocytes into a highly immunodeficient non-human animal;

(b) detecting the proliferation of lymphocytes at the site of transplantation; and

(c) recovering cells comprising lymphocytes from the site of transplantation;

(27) the method of (26), further comprising the step of:

(d) culturing the recovered cells comprising lymphocytes in vitro to further proliferate the lymphocytes;

(28) the method of (26) or (27), wherein the lymphocytes comprise plasma cells;

(29) the method of any one of (26) to (28), wherein the lesion tissue is a cell forming a cancer or a hyperplasia, or a virus-infected cell;

(30) a therapeutic composition against a lesion tissue, wherein the composition is produced according to the method of any one of (26) to (29);

(31) an antibody against an abnormal cell comprised in a lesion tissue, wherein the antibody is comprised in a serum recovered from a highly immunodeficient non-human animal transplanted with a lesion tissue comprising plasma cells, blood comprising plasma cells, or plasma cells recovered from a lesion tissue or blood; (32) the antibody of (31), which is a polyclonal antibody; and (33) a therapeutic or diagnostic composition against a lesion tissue, wherein the composition comprises a nucleic acid of (17) or (18), or an antibody of any one of (19) to (25), (31), and (32) as an active ingredient.

Effects of the Invention

According to the present invention, plasma cells, which produce antibodies that recognize abnormal cells (such as cancer cells and abnormal cells forming benign hyperplasia) in polyclonal cell groups such as transplanted tissue fragments, can be selectively proliferated by transplanting lymphocyte-infiltrated lesion tissues into highly immunodeficient animals, and the plasma cells of interest can be easily separated. This easy separation of plasma cells further facilitates or enables the acquisition of antibodies recognizing antigens specific to lesion tissues and nucleic acids encoding these antibodies from the plasma cells. Moreover, plasma cells, antibodies, or nucleic acids which encode the antibodies acquired by the present invention contribute as novel therapeutic or diagnostic agents against lesion tissues.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows photographs of HE-stained paraffin sections prepared after thinly slicing human breast cancer tissues. Equal amounts of human breast cancer tissues were transplanted into NOG mice and SCID mice, and the mice were dissected nine weeks later. A high degree of accumulation of plasma cells is observed in NOG mice. Moreover, an image of leukocytes infiltrating tumor cells is observed, suggesting that the immune system is actively functioning. These tissue images strongly suggested the presence of a cancer-specific immune response.

FIG. 2 is a graph showing the results of transplanting human breast cancer tissues into NOG mice and SCID mice and monitoring the changes in human IgG antibody titer. IgG antibody titers in NOG mice showed values that were ten to hundred times higher than those in SCID mice.

FIG. 3 shows the results of transplanting specimens from human prostate cancer and benign prostatic hyperplasia into NOG mice and monitoring the changes in human IgG and IgM antibody titers. An increase in antibody titer was observed in four (shown in the figure) out of the 40 transplanted specimens. RNAs were extracted from four of these cases and the antibody genes were amplified.

FIG. 4 shows the results of transplanting human breast cancer specimens into NOG mice and monitoring the changes in human IgG and IgM antibody titers. An increase in antibody titer was observed in four specimens shown in the figure among the ten specimens. RNAs were extracted from four of these cases and the antibody gene was amplified.

FIG. 5 is a graph showing the degree of accumulation of plasma cells versus the concentration of human IgG in the serum of NOG mice. There was a good correlation between the degree of accumulation (density) and the antibody titer.

FIG. 6 is a graph showing the half-life of human IgG after administration to NOG mice and SCID mice. The half-life in NOG mice was about 18 days, while that in SCID mice was 21 days. The half-life in NOG mice was slightly shorter. This indicated that the high titer of human antibodies in NOG mice was not caused by a delay in clearance.

FIG. 7 shows results of a FACS investigation of whether human antibodies comprised in the serum of NOG mice transplanted with benign prostatic hyperplasia specimens recognize surface antigens on the prostate cancer cell line DU145. As is clear from the results, IgG antibodies recognizing the cancer cell line were present among IgG antibodies in the serum of NOG mice transplanted with benign prostatic hyperplasia.

FIG. 8 shows results of a FACS investigation of whether human antibodies present in the serum of NOG mice transplanted with breast cancer (ductal carcinoma) specimens recognize surface antigens on the ductal carcinoma cell line ZR-75-1, As is clear from the results, IgM antibodies recognizing the carcinoma cell line were present among IgM antibodies in the serum of NOG mice transplanted with breast cancer.

FIG. 9 shows a confirmation by flow cytometry of the process by which phages presenting scFv are concentrated using binding to the prostate cancer cell line DU145 as an index. The amount of phages which bind to DU145 cells increased with the increase of the number of rounds of concentration and selection.

FIG. 10 shows a confirmation by flow cytometry of the binding of DU145 cells and DU145 cell-binding clones when these clones were isolated from a library after five or six cycles of concentration and selection.

FIG. 11 is a photograph showing a silver staining of Protein A-purified scFv fusion proteins following separation by SDS-PAGE.

FIG. 12 is a graph showing a confirmation by flow cytometry of the binding of recombinant 5-16scFv Fc fusion proteins to DU145 cells.

FIG. 13 shows a flow cytometry analysis after staining cancer cell lines using human antibodies that appear in the serum of NOG mice transplanted with stomach cancer tissues. Human IgM antibodies in the serum of mice transplanted with PLR0631 reacted with the human stomach cancer cell line AGS in a concentration-dependent manner (a). In addition, the serum of mice transplanted with PLR0624 reacted with the human stomach cancer cell line SNU-1 (b).

FIG. 14 shows photographs of tissue staining of cancer tissues using human antibodies present in mouse serum. a: Reactivity of IgMs in the serum of mice transplanted with PLR0659 stomach cancer tissues with a colorectal cancer cell line; be Reactivity of IgMs in the serum of mice transplanted with PLR stomach cancer tissues with a stomach cancer cell line. The cell membrane of cancer cells indicated by the arrows was stained.

FIG. 15 shows an observation by flow cytometry of the staining of the cancer cell line AGS by human IgGs (a) and IgMs (b) from the serum of mice transplanted with PLR0530 stomach cancer tissue. Nearly the same staining properties were observed with antibody concentrations of 50 μg/ml and 10 μg/ml.

FIG. 16 is a graph showing a confirmation by flow cytometry of the binding of AGS cells to AGS cell-binding clones when these clones were isolated from a concentrated, selected library.

FIG. 17 is a photograph showing a silver staining of a Protein A-purified scFv fusion protein following SDS-PAGE separation.

FIG. 18 is a graph showing a confirmation by flow cytometry of recombinant fusion proteins 1-3 scFv Fc that are bound to AGS cells.

FIG. 19 shows an immunohistological staining of cancer tissues using chimeric antibodies. Tissues excised from stomach cancer patients (a and c), tissues excised from a duodenum cancer (b), and tissues excised from the colon (CRC) (d) were used as cancer tissues. Immunostaining confirmed that the chimeric antibodies react with the cytoplasm of stomach cancer cells, and with the luminal side of duodenum cancer and colon cancer cell membranes.

DETAILED DESCRIPTION

As a first aspect, the present invention provides a method of proliferating plasma cells, where the method comprises the step of transplanting tissues comprising plasma cells into a highly immunodeficient non-human animal.

Herein, “plasma cells” refer to cells which can produce antibodies, and the antibody class is not particularly restricted. Thus, the term “plasma cells” used in the present specification comprises: B cells in the early stages of B cell differentiation, expressing a μ chain on the cell surface as antigen receptor; B cells in which the transcription process has changed and IgM production has changed from membrane-type IgMs to secreted-type IgMs; mature B cells that have completed class-switching and secrete IgGs, IgAs, and IgMs; and B cells in the final stages of differentiation, capable of producing 2000 IgG molecules per second. In addition, the “proliferation of plasma cells” referred to herein comprises both the proliferation and differentiation of the aforementioned B cells.

Examples of tissues comprising plasma cells include cells and tissues containing substances that may be recognized as foreign matter by the body's immune system or cells and tissues containing degeneration products of organisms or biological substances, such as neoplasms. Examples of such comprise tissues forming a cancer or hyperplasia and cells infected with viruses. Since such cancers and virus-infected cells may form lesion sites in the body, tissue fragments from lesion sites of patients can be directly used as “plasma cell-comprising tissues”. For example, the following types of lesions are preferable as “plasma cell-comprising tissues”.

Solid cancer lesions

Blood cancer lesions

Hyperplasia lesions

Arteriosclerosis lesions

Inflammatory disease lesions

Metabolic disease lesions

Lesions formed by infectious pathogens

Autoimmune disease lesions

In particular, solid cancer lesions and hyperplasia lesions are preferable as the aforementioned tissues. Examples of solid cancer lesions include lesions of prostate cancer, stomach cancer, breast cancer, lung cancer, liver cancer, colorectal cancer, and pancreatic cancer. Lesions forming benign hyperplasia, particularly lesions fanning benign prostatic hyperplasia are preferable as hyperplasia lesions. These tissues can be collected by surgical excision. For example, cancer tissues collected for examination by biopsy can be used as lesion tissues in the present invention. In addition, tissues excised from patients by surgical excision as a surgical treatment are also useful as lesion tissues.

Moreover, secondary inflammatory diseases are comprised in the inflammatory diseases. Examples of metabolic diseases include Alzheimer's disease that forms amyloid plaques.

Examples of infectious pathogens include, but are not limited to, HCV (human hepatitis C virus), HBV (human hepatitis B virus), and HIV (human immunodeficiency virus). Tissues or cells invaded by infectious pathogens such as these viruses can be collected by biopsy or from the blood.

In addition to lesion sites derived from patients, those artificially formed in laboratory animals and the like may also be used as the “plasma cell-comprising tissues”. Herein, examples of lesion sites artificially formed in laboratory animals include those formed by artificially transplanting heterologous cells or tissues into animals, and those formed by expressing an artificially-introduced exogenous gene either systemically or at a specific sites such as in tissues. Moreover, lesion tissues can also be formed by infecting laboratory animals with viruses.

The aforementioned “plasma cell-comprising tissues” are indicated as an example of a most typical sample when collecting lymphocytes and plasma cells as starting cells to be proliferated. However, not only lymphocytes and plasma cells that are infiltrating tissues such as lesions, but also lymphocytes and plasma cells present in blood or those present separated from such tissues or blood, may be used as starting cells. Although the terms “plasma cell-comprising (or plasma cell-infiltrated) tissues” and “lymphocyte-comprising (or lymphocyte-infiltrated) tissues” are used below in the present specification to indicate samples serving as starting cells to proliferate plasma cells, these terms encompass blood comprising plasma cells and the like, or plasma cells themselves separated from tissues or blood. Thus, tissues or blood comprising plasma cells and the like or plasma cells and such separated from these tissues or blood may be used in transplantations into the highly immunodeficient non-human animals described below. A “highly immunodeficient non-human animal” indicates an animal having an activity that can proliferate plasma cells from transplanted tissues without rejecting the transplanted tissues or cells, examples of which include non-human animals not possessing T cells, B cells, and NK cells and demonstrating a low IFN production ability, specifically NOG mice. Although examples using mice are indicated in the present application, examples of non-human animals other than mice include monkeys, pigs, dogs, rabbits, guinea pigs, and rats. Furthermore, hereinbelow in the present specification, “highly immunodeficient non-human animals” may simply be referred to as “highly immunodeficient animals” for convenience.

There are no particular limitations on transplantations into highly immunodeficient non-human animals, provided that the site of transplantation allows the proliferation of plasma cells; however, the transplantation can be carried out subcutaneously as that would be convenient for transplantation procedures and subsequent collection. Here, the transplanted plasma cells proliferate predominantly at the sites of transplantation without requiring any particular selection pressure. The present inventors discovered that this degree of plasma proliferation (or degree of accumulation) closely correlates with the antibody titer in the serum of the highly immunodeficient animals (antibody titer of antibodies derived from transplanted tissues). Consequently, whether or not plasma cells at the site of transplantation in the highly immunodeficient animals have proliferated can be verified by measuring the antibody titer in the serum collected from the animals. There are no limitations on the type of antibody measured, provided that a correlation with plasma cell proliferation can be observed; however, the antibodies are preferably IgMs or IgGs. Antibody titer can be measured by a method widely known to those skilled in the art. For example, IgMs or IgGs can be measured by selecting a method from among known methods such as single radial immunodiffusion (SRID), turbidimetric immunoassay (TIA), laser nephelometry, latex agglutination (LA), RIA, EIA, and ELISA. Use of commercially available assay kits enables easy and convenient measurement.

As the number of antibody-producing cells is increased at a site of transplantation in highly immunodeficient animals, the above-described present invention makes it easy to separate antibody-producing cells, which was difficult in the past. It also facilitates the production and such of antibodies against the lesion tissues described below.

As a second aspect, the present invention provides a method for producing antibody-producing cells. As previously described, the present inventors discovered that, when lesion tissues are transplanted into highly immunodeficient animals such as NOG mice, plasma cells infiltrating the lesion tissues can be advantageously proliferated. Thus, by using highly immunodeficient animals as a means for producing plasma cells, it becomes possible to amplify and recover the plasma cells, which were obtainable only in trace amounts in the past. Namely, the method of producing antibody-producing cells of the present embodiment comprises the steps of (a) transplanting a lesion tissue comprising infiltrating lymphocytes into a highly immunodeficient non-human animal; (b) detecting the proliferation of plasma cells at the site of transplantation; and (c) recovering the lesion tissue comprising the plasma cells from the site of transplantation.

Herein, the step of transplantation and the step of detecting the proliferation of plasma cells can be carried out in the same manner as in the aforementioned method of proliferating plasma cells. Recovery of the proliferated plasma cells may be carried out by recovering, from the site of transplantation, the transplanted tissue itself in which plasma cells have proliferated, or by selectively recovering the plasma cells. Microdissection is an example of a means for selectively recovering plasma cells. Microdissection is a technique for excising specific cells from a tissue section. For example, target cells can be isolated from frozen tissue sections using the Laser Microdissection (LMD) system. A system for excising tissue sections with an ultraviolet laser is commercially available. The use of this system, which involves specifying the region to be excised on a computer image under microscopic observation, makes it possible to excise any region from a tissue section.

A large number of plasma cells can be isolated by observing a specimen under a microscope and selecting a portion enriched with plasma cells. Specific plasma cells can be easily acquired by microdissection of single plasma cells.

The plasma cells recovered from the site of transplantation of highly immunodeficient animals are increased as compared to plasma cells in lesion tissues collected from patients and the like. As indicated in the forthcoming Examples, the increase in the number of plasma cells is accompanied by an increase in the titer of antibodies against the lesion tissues. Since plasma cells recovered in this manner produce antibodies against the lesion tissues more actively, these plasma cells can be effectively used as materials for obtaining antibodies or genes thereof, or the plasma cells themselves can be effectively used as a therapeutic composition for (treating) lesion tissues. Furthermore, when using the recovered plasma cells as a means for producing antibodies and the like, they are preferably fused with partner cells such as mouse or human myeloma cells to establish an antibody-producing cell line.

As a third aspect, the present invention provides a method of producing nucleic acids encoding antibodies or portions thereof. As previously described, plasma cells can be advantageously proliferated at a site of transplantation by transplanting lesion tissues infiltrated with lymphocytes into highly immunodeficient animals. Since such plasma cells that proliferated at a site of transplantation have an ability to produce antibodies against abnormal cells included in the lesion tissues, plasma cells recovered from the site of transplantation are a preferable cloning source of nucleic acids encoding antibodies against abnormal cells, or portions of these nucleic acids. In short, the method of the present invention for producing a nucleic acid encoding an antibody comprises the steps of: (a) transplanting a lesion tissue comprising infiltrating lymphocytes into a highly immunodeficient non-human animal; (b) detecting the proliferation of plasma cells at the site of transplantation; (c) recovering the lesion tissue comprising plasma cells from the site of transplantation; and (d) recovering the nucleic acid encoding the antibody from the recovered lesion tissue.

Transplantation of lesion tissues comprising infiltrating lymphocytes into highly immunodeficient non-human animals and detection of plasma cell proliferation at the site of transplantation can be carried out as in the aforementioned proliferation method and the like. Moreover, recovery of plasma cells from the site of transplantation may be carried out by recovering the lesion tissues themselves in which plasma cells have proliferated, from the site of transplantation or by selectively recovering plasma cells by microdissection and the like, as in the aforementioned method for producing plasma cells.

As a method for acquiring nucleic acids encoding antibodies, or portions thereof, from recovered lesion tissues or from selectively recovered plasma cells, chromosomes may be isolated from plasma cells or transcripts thereof and an antibody gene or a portion thereof may be obtained therefrom. However, since antibody genes obtainable from plasma cells are extremely small in amount, it is convenient to obtain the antibody gene, or portion thereof, after amplification. Methods for amplifying genes are known in the art. For example, the PCR method is preferred as a method for amplifying antibody genes. A method for isolating antibody genes using the PCR method is described below.

First, mRNAs are extracted from isolated plasma cells (B cells). cDNAs are synthesized by using the extracted mRNAs as a template to obtain a cDNA library. Commercially available kits are conveniently used for extracting mRNAs and for constructing the cDNA library. In this invention, mRNAs derived from a small number of plasma cells are used. In practice, mRNAs obtained from only few cells are extremely small in amount, and have low yields when directly purified. Therefore, mRNAs are usually purified after the addition of carrier RNAs that clearly contain no antibody genes. Alternatively, when a certain amount of RNA can be extracted, efficient extraction is possible even with only the RNAs of antibody-producing cells. The addition of carrier RNAs may not be required for extracting RNAs from, for example, 10 or more, 30 or more, preferably 50 or more antibody-producing cells.

By using the cDNA library thus obtained as a template, antibody genes can be amplified by the PCR method. Primers for amplifying antibody genes by the PCR method are known in the art. For example, primers for amplifying human antibody genes can be designed based on disclosures in research papers (J. Mol. Biol. (1991) 222, 581-597) and web sites (mrc-cpe.cam.ac.uk). These primers have different nucleotide sequences depending on the immunoglobulin subclass. Accordingly, when a cDNA library with an unknown subclass is used as a template, the PCR method is performed considering all possible immunoglobulin subclasses.

For example, to obtain genes encoding human IgG, primers that allow the amplification of genes encoding γ1 to γ5 as the heavy chain, and κ chain and λ chain as the light chains, can be used. For amplifying genes of the IgG variable region, a primer capable of annealing to a portion that corresponds to the hinge region is generally used as the 3′ primer. An example of such a primer is the primer of SEQ ID NO: 55. A primer corresponding to each subclass, such as the primers shown in the Example 2 of the present application, can be used as the 5′ primer.

The antibody gene or portion thereof can also be amplified directly, without the intermediary isolation of cDNAs, by RT-PCR using the above primers and mRNAs collected from plasma cells.

PCR products obtained using primers for amplifying genes of the respective heavy and light chain subclasses are considered as independent libraries. Using thus synthesized libraries, it is possible to reconstitute antibodies or portions thereof by combining the heavy chains and light chains.

As mentioned above, nucleic acids encoding “antibodies or portions thereof” are produced in the present invention. The nucleic acids may encode a whole antibody or an antibody portion. The antibodies are preferably IgGs or IgMs. Examples of preferable partial fragments of an antibody comprise Fab, F(ab′)², and Fv which comprise variable regions equipped with the complementarity determining regions (CDRs) of the antibody.

As mentioned above, nucleic acids encoding the variable region of an antibody are preferred antibody fragments of the present invention. A complete immunoglobulin molecule can be reconstituted by obtaining nucleic acids encoding a variable region and linking the nucleic acids with nucleic acids encoding a constant region. Constant regions of antibodies within the same class have approximately the same structure. That is, the structure of the constant region has no effect on the antigen-binding activity. Accordingly, if the structure of the variable region of an antibody can be elucidated, antibodies having similar activity can be reconstituted through conjugation with a constant region that is already obtained.

Moreover, nucleic acids encoding antibodies, or portions thereof, of the present invention comprise genetically recombinant antibodies whose structures have been artificially modified. For example, they comprise single chain Fv (scFv) in which the variable regions of a heavy chain and light chain are linked by a linker. scFv can be obtained by ligating the V regions of the antibody H chain and L chain. In the scFv, the V regions of the H chain and L chain are ligated via a linker, and preferably via a peptide linker (Huston, J. S. et al., Proc. Natl. Acad. Sci. U.S.A (1988) 85, 5879-5883). Examples of the V regions of the H chain and L chain in the scFv are shown in the Examples of the present application, but are not limited thereto.

The peptide linker used to ligate the V regions may be any single-chain peptide comprising 12 to 19 residues. As shown in the scFv preparation example in Example 3, DNAs encoding scFv are obtained by: using as template a DNA encoding the entirety or a desired amino acid sequence of a DNA encoding the H chain or H chain V region or a DNA encoding the L chain or L chain V region of an aforementioned antibody; amplifying by PCR using a primer pair which defines both ends; then amplifying after combining a DNA encoding a peptide linker portion and a primer pair which defines both ends such that each end is linked to a H chain or L chain. Moreover, once DNAs encoding scFv are produced, expression vectors comprising them and hosts transformed with the expression vectors can be obtained following routine procedure.

Furthermore, in the case of antibody genes acquired in mammals and such other than humans, non-human animal-human chimeric antibody genes, in which the constant region genes is substituted with that of humans, and humanized antibody genes, which are formed by transplanting CDRs that constitute the variable regions of mammals other than humans into human variable regions, are also comprised in the antibody genes of the present invention. In addition, nucleic acids encoding antibodies in the present invention can also comprise artificial structures such as PNA, provided that their nucleotide sequences are maintained.

As a fourth aspect, the present invention provides a method for producing antibodies against abnormal cells contained in lesion tissues.

When the antibodies are polyclonal antibodies, they can be easily prepared by collecting blood from highly immunodeficient animals transplanted with lesion tissues comprising plasma cells, blood comprising plasma cells, or plasma cells recovered from lesion tissues or blood, and separating the serum. As also indicated in the Examples described below, antibodies against abnormal cells contained in lesion tissues were detected in highly immunodeficient animal blood when the lesion tissues were transplanted into highly immunodeficient animals and blood was collected from the animals. Thus, a method for preparing polyclonal antibodies against abnormal cells contained in lesion tissues can be carried out by separating serum from highly immunodeficient animals transplanted with lesion tissues.

Another method for producing antibodies is the method of preparing them from the aforementioned plasma cells produced based on lesion tissues or from fused cell lines of plasma cells and partner cells. Examples of partner cells include mouse myeloma cells and human myeloma cells. Antibody-producing cell lines which produce monoclonal antibodies can be prepared by fusing partner cells with cloned plasma cells. Isolation and purification of target antibodies against abnormal cells present in lesion tissues such as cancer from such fusion cell lines of plasma cells and partner cells can be carried out by affinity chromatography and such using, for example, the binding activity to abnormal cells of cancer and such, or to their surface molecules. Moreover, in a different method for producing antibodies, antibodies are artificially produced based on genes encoding the aforementioned antibodies or portions thereof. Specifically, this method comprises the steps of: introducing, into an expression vector, nucleic acids encoding the aforementioned antibodies or portions thereof, or nucleic acids in which the nucleic acids have been chimerized or humanized; transforming host cells with vectors carrying the aforementioned nucleic acids; and producing antibodies by culturing the transformants.

Expression vectors that can be used herein need to comprise units that regulate the transcription and translation of genetic information, such as promoters and terminators. For example, when microorganisms belonging to the Escherichia genus such as E. coli are used as hosts, plasmids of the pBR or pUC series can be used as plasmid vectors, and any promoters selected from those such as lac, trp, tac, trc, λ phage PL, and PR can be used. Terminators may originate from trpA, phage, and rrnB ribosomal RNA.

When the hosts are Bacillus microorganisms such as B. subtilis, plasmids such as those of the pUB110 and pC194 series can be used, and genes may be integrated into chromosomes in some cases. Promoters and terminators may be derived from apr, npr, amy, and such.

Examples of other prokaryotic cells comprise microorganisms such as Pseudomonas (e.g. P. putida, P. cepacia; pKT240 vectors, and such), Brevibacteria (e.g. B. lactofermentum; pAJ43), Corynebacteria (e.g. C. glutamicum; pCS11, pCB101), Streptococcus (e.g. pHV1301, pGK1), Lactobacillaceae (e.g. pAMI31), Rhodcoccus (e.g. plasmids isolated from R. rhodochrous (J. Gen. Microbiol, 138: 1003 (1992)), Streptomyces (e.g. S. lividans, S. virginiae; pIJ486, pKC1064, pUWL-KS), Enterobacter, Erwinia, Klebsiella, Proteus, Salmonella (e.g. S. typhimurium), Serratia (e.g. S. marcescans), and Shigella.

Among expression systems utilizing eukaryotic microorganisms, a system using Saccharomyces cerevisiae as a host, and plasmids from YRp, YEp, YCp, and YIp series is known. Therein, promoters and terminators such as ADH, GAPDH, PHO, GAL, PGK, and ENO can be used. Other microorganisms used in the expression vector systems of the present invention comprise Kluyveromyces (e.g. K. lactis; plasmids of the 2 μm, pKD1, pGKI1, and KARS series, and such), Schizosaccharomyces (e.g. S. pombe; pAUR224), Zygosaccharomyces (e.g. Z. rouxii; pSB3 and PH05 promoters from S. cerevisiae), Hansenula (e.g. H. polymorpha), Pichia (e.g. P. pastoris), Candida (e.g. C. maltosa, C. tropicalis, C. utilis, and C. albicans), Aspergillus (e.g. A. oryzae, A. niger), and Trichoderma (e.g. T. reesei),

In another embodiment, plant cells may be used as hosts. For example, hosts may be plant cells derived from cotton, corn, potato, tomato, soybean, petunia, tobacco, and such. A particularly well-known system uses cells derived from Nicotina tabacum cultured as a callus. To transform plant cells, expression vectors such as pMON530 are introduced into bacteria such as Agrobacterium tumefaciens. By infecting tobacco (e.g. Nicotina tabacum) with these bacteria, desired polypeptides can be obtained from the tobacco leaves.

Cells from insects such as silkworms (Bombyx mori), mosquitoes (e.g. Aede aegypti, Aedes albopictus) and fruit flies (Drosophila melanogaster) can be used as hosts. For example, when using silkworms as hosts, DNAs encoding antibodies may be inserted into baculovirus vectors and such, these vectors may be used to infect silkworms, and desired polypeptides can be obtained from silkworm body fluids (Nature 315: 592-594 (1985)).

Examples of expression vectors when using animal cells as hosts comprise pME18S (Med. Immunol. 20: 27-32 (1990)), pEF-BOS (Nucleic Acids Res. 18: 5322 (1990)), pCDM8 (Nature 329: 840-842 (1987)), pRSVneo, pSV2-neo, pcDNAI/Amp (Invitrogen), pcDNAI, pAMoERC3Sc, pCDM8 (Nature 329: 840 (1987)), pAGE107 (Cytotechnology 3: 133 (1990)), pREP4 (Invitrogen), pAGE103 (J. Biochem. 101: 1307 (1987)), pAMoA, pAS3-3, pCAGGS (Gene 108: 193-200 (1991)), pBK-CMV, pcDNA3.1 (Invitrogen), and pZeoSV (Stratagene).

Promoters may be cytomegalovirus IE gene promoter and enhancer, SV40 early promoter, retrovirus LTRs such as those from RSV, HIV, and MMLV, and gene promoters from animal cells such as metallothionein, β-actin, elongation factor-1, HSP genes, and such. Alternatively, viral vectors such as those mentioned above may also be used. Viral vectors may be derived from DNA viruses and RNA viruses such as retroviruses, adenoviruses, adeno-associated viruses, herpes viruses, vaccinia viruses, poxviruses, Sindbis viruses, Sendai viruses, SV40, and HIV.

Host cells among animal cells may be mouse myeloma cells (e.g. SP2/0, NSO), rat myeloma cells (e.g. YB2/0), mouse hybridoma cells, Namalwa cells (including KJM-1 cells and such), human embryonic kidney cells (e.g. 293 cells), human leukemia cells (e.g. BALL-1), CHO cells, COS cells (e.g. COS-1, COS-7), hamster embryonic kidney cells (e.g. BHK), mouse Sertoli cells (e.g. TM4), African green monkey kidney cells (e.g. VERO-76), HBT637 cells, HeLa cells, rabbit kidney cells (e.g. MDCK), human liver cells (e.g. HepG2), mouse mammary tumor cells (e.g. MMT060562 cells), TR1 cells, MRC cells, FS3 cells, etc.

Methods for introducing expression vectors depend on the type of host cell and vector, but any method can be used as long as it allows introduction of antibody-encoding DNA into cells. Vectors can be introduced into prokaryotic cells by methods utilizing calcium ions (Proc. Natl. Acad. Sci, USA 69: 2110 (1972)), protoplasts (Japanese Patent Application No. (JP-A) S63-24829 (unexamined, published Japanese patent application)), electroporation (Gene 17: 107 (1982); Molecular & General Genetics 168: 111 (1979)), and such. Vectors can be introduced into yeast cells by electroporation (Methods in Enzymology, 194: 182 (1990)), spheroplasts (Proc. Natl. Acad. Sci. USA 81: 4889 (1984)), lithium acetate (J. Bacteriol. 153: 163 (1983))), and such. Vectors can be introduced into plant cells by using Agrobacterium (Gene 23: 315 (1983); WO 89/05859), sonication (WO 91/00358), and such. Vectors can be introduced into animal cells by using electroporation (Cytotechnology 3: 133 (1990)), calcium phosphate (JP-A H02-227075), lipofection (Proc. Natl, Acad, Sci. USA 84: 7413 (1987); Virology 52: 456 (1973)), co-precipitation with calcium phosphate, DEAE-dextran, direct injection of DNA using microcapillaries, and such.

Transformants obtained as described above can be cultured, for example, by the following methods:

Culture media for transformants of prokaryotes and eukaryotic microorganisms can be natural or synthetic, as long as the media allows efficient culture of the transformants, and comprises nutrients utilizable by the organisms and essential for their growth, such as carbon and nitrogen sources, and inorganic salts. Culture may be carried out under aerobic or anaerobic conditions, and other conditions such as temperature, pH of the medium and duration of the culture can be determined appropriately by one skilled in the art, depending on the type of transformant. When using expression vectors equipped with inducible promoters, inducers may be added to the medium as necessary. For example, expression of vectors comprising the lac promoter can be induced by adding IPTG; and expression of vectors comprising the trp promoter can be induced by adding IAA as an inducer.

When using insect cells as host cells, a medium such as the TNM-FH medium (Pharmingen), Sf-900 II SFM (Life Technologies), ExCell400 and ExCell405 (JRH Biosciences), and Grace's Insect Medium (Nature 195: 788 (1962)) can be used. If necessary, antibiotics such as gentamicin may be added to the medium.

For animal cell transformants, common media such as RPMI1640 (The Journal of American Medical Association 199: 519 (1967)), Eagle's MEM (Science 122: 501 (1952)), DMEM (Virology 8: 396 (1959)), and 199 medium (Proceeding of the Society for the Biological Medicine 73: 1 (1950)), or such media added with BSA and the like, can be used. Culture can be carried out under normal conditions such as pH 6 to 8, 30° C. to 40° C., and 5% CO₂. If necessary, antibiotics such as kanamycin and penicillin may be added to the medium.

The antibodies of the present invention obtained as above can be isolated from within host cells, or from the culture medium if secreted into the extracellular space using signal sequences. They can then be purified as substantially pure polypeptides. The antibodies of the present invention can be separated or purified by appropriately selecting, or combining as necessary, methods generally used in separation and purification. Such methods can be chromatography, filtration, ultrafiltration, salting out, solvent precipitation, solvent extraction, distillation, immunoprecipitation, SDS-polyacrylamide gel electrophoresis, isoelectric focusing electrophoresis, dialysis, and recrystallization. Chromatography comprises affinity chromatography, ion exchange chromatography, hydrophobic chromatography, gel filtration, reverse phase chromatography, absorption chromatography, and the like (Strategies for Protein Purification and Characterization: A Laboratory Course Manual, Daniel R. Marshak et al. eds., Cold Spring Harbor Laboratory Press (1996); Antibodies: A Laboratory Course Manual, Harlow and David Lane eds., Cold Spring Harbor Laboratory Press (1988)). Such chromatographies may be performed using liquid chromatographies such as HPLC, FPLC, and the like. In addition, the antibodies of the present invention may be purified by making use of their affinities towards antigens.

Furthermore, the antibodies obtained by the methods of the present invention may be partial fragments of antibodies or modified antibodies. For example, the antibody fragments may be expressed from nucleic acids encoding Fab, F(ab′)2, Fv, single chain Fv (scFv), in which Fv from H or L chains are ligated by an appropriate linker and such via the aforementioned expression vectors and hosts (see, for example, Co, M. S. et al., J. Immunol. (1994) 152, 2968-2976; Better, M. & Horwitz, A. H. Methods in Enzymology (1989) 178, 476-496, Academic Press, Inc.; Plueckthun, A. & Skerra, A. Methods in Enzymology (1989) 178, 476-496, Academic Press, Inc.; Lamoyi, E., Methods in Enzymology (1989) 121, 663-669; and Bird, R. E. et al., TIBTECH (1991) 9, 132-137). Moreover, the antibody fragments can be obtained by expressing full-length antibodies, then treating the antibodies with enzymes such as papain and pepsin to produce antibody fragments.

Antibodies bound to various types of molecules, such as polyethylene glycol (PEG), may be used as modified antibodies. Furthermore, antibodies may bind to radioisotopes, chemotherapeutics, cytotoxic substances such as bacteria-derived toxin, and labeling substances. Such modified antibodies can be obtained by chemically modifying the resulting antibodies. Methods for modifying antibodies are already established in the art. The term “antibody” in the present invention also encompasses the modified antibodies as described above.

Furthermore, the antibodies of the present invention may be bispecific antibodies. The bispecific antibodies may have antigen-binding sites recognizing different epitopes on the antigen molecules, or may have one antigen-binding site recognizing antigens and the other recognizing a cytotoxic substance such as a radioactive substance, chemotherapeutic agent, and cell-derived toxin. In this case, it is possible to inhibit the growth of cancer cells by directly applying the cytotoxic substance to the cells expressing antigens to specifically damage them. Bispecific antibodies can be prepared by linking HL pairs of two kinds of antibodies, or obtained by fusing hybridomas that produce different monoclonal antibodies to prepare fused cells generating bispecific antibodies. Furthermore, bispecific antibodies can be generated by using genetic engineering techniques.

Techniques common to the field of genetic engineering can be used to carry out procedures for constructing an expression system for producing the antibodies of the present invention, and for constructing recombinant vectors appropriate for the hosts (see for example, Sambrook et al., Molecular Cloning, Cold Spring Harbor Laboratories (1989)). Host cells may be prokaryotic cells such as bacteria, and eukaryotic cells such as yeast, animal cells, insect cells, and plant cells, as long as the cells are capable of expressing the light chains of the present invention or the antibodies comprising the light chains. Mammalian cells are particularly preferred in view of glycosylation.

Whether or not the antibodies produced as described above are the desired antibodies can be confirmed using as an index the binding activity to abnormal cells in a lesion, or to their surface molecules. Specifically, antibodies obtained by the aforementioned methods are contacted with cancer cells and whether or not the aforementioned cancer cells and antibodies bind is analyzed. Herein, the antibodies that bind to the cancer cells are confirmed to be the desired antibodies in the present invention.

In the above description, there are no particular limitations on the method for detecting the binding between the antibodies and cancer cells, and any method can be used. For example, an immobilized cancer specimen is reacted with a test antibody, and then with a labeled antibody which recognizes the test antibody. The binding of the test antibody to cancer cells can be confirmed by detecting the labeled antibody on the immobilized specimen after washing. Enzymatically active proteins such as peroxidase and β-galactosidase, and fluorescent substances such as FITC can be used as the label. Moreover, flow cytometry is also a preferable method for detecting the aforementioned binding. Alternatively, the binding of the antibody to cancer cells can be detected without any labeling by using a method that uses surface plasmon resonance (SPR), for example the commercially available BIACORE system. Cancer tissues to be analyzed for antibody-binding activity may be cancer tissues forming the lesion from which plasma cells (B cells) are obtained. Alternatively, cancer tissues of the same organ which have been removed from different individuals and cell lines derived from cancers can be also used. Furthermore, cancer tissues derived from different organs, cell lines derived from cancers, cancer cell lines equipped with specific surface antigens, or such can also be used to screen for antibodies which specifically or commonly react with different types of cancers.

In the above description, an antibody whose reactivity towards a cancer tissue is significantly high compared to the normal tissue is said to bind specifically to the cancer. For comparing the reactivities of the antibodies of the present invention, the same type of tissue is generally used. That is, the reactivity of an antibody is compared between a cancer tissue and a normal tissue of the organ from which the cancer tissue is derived. Under conditions in which an antibody's reactivity towards a cancer tissue can be confirmed, the antibody is said to have a specific reactivity towards the cancer tissue when no binding activity towards the normal tissue can be detected.

Methods of screening for antibodies using binding activity as an index include the panning method which utilizes phage vectors. When the obtained antibody genes are gene libraries of heavy and light chain subclasses as described above, screening methods that use phage vectors are advantageous. As described in the Examples, genes encoding variable regions of the heavy and light chains can be made into single chain Fv (scFv) through conjugation with a suitable linker sequence. Libraries expressing scFv on phage surfaces can be obtained by inserting a scFv-encoding gene into a phage vector. By contacting these phages with an antigen of interest and recovering the phages bound to the antigen from the library, DNAs encoding scFv with the desired binding activity can be recovered. scFv having the desired binding activity can also be concentrated by repeating this procedure as necessary. For example, Barabas, III, C. F. et al., “Phage Display—A Laboratory Manual”, Cold Spring Harbor Laboratory Press, 2001, can be referred to regarding the preparation of phage libraries. Moreover, commercially available systems for constructing phage libraries can be used for preparing phage libraries, and preparation can be carried out by using, for example, pCANTAB phagemid vector or M13K07 helper vector as in the Examples.

The aforementioned antibodies of the present invention are useful for the diagnosis and treatment of lesion tissues. When using antibodies of the present invention for diagnosis, the antibodies can be used as antibody molecules labeled with a traceable label such as an enzyme label, a radioactive label, or a fluorescent label. The presence of cancer may be detected from the location of the antibodies after administering the antibodies modified with such a label to subjects. Moreover, the antibodies of the present invention can also be immobilized onto a solid phase such as a plate or beads to form a diagnostic kit and the like. Furthermore, the case of using the antibodies of the present invention for treatments is described later.

As a fifth aspect, the present invention provides a method for producing therapeutic compositions against lesion tissues. Since plasma cells that proliferate and are activated in the highly immunodeficient animals by the aforementioned methods of the present invention produce antibodies to abnormal substances within lesion tissues, these cells can be used as a therapeutic composition against the lesion tissues. Consequently, the aforementioned method of the present invention for producing plasma cells can also be applied as a method for producing therapeutic compositions against lesion tissues. Namely, the method of the present invention for producing therapeutic compositions against lesion tissues comprises the steps of: (a) transplanting a lesion tissue infiltrated with lymphocytes to a highly immunodeficient non-human animal; (b) detecting lymphocyte proliferation at the site of transplantation; and (c) recovering cells comprising lymphocytes from the site of transplantation.

The “lesion tissues infiltrated with lymphocytes” in the production of therapeutic compositions are the same as in the aforementioned methods for proliferating and producing plasma cells, and are cells and tissues having substances that may be recognized as foreign matter by the body's immune system or having degeneration products of organisms or biological substances, such as neoplasms. Examples of such include tissues forming a cancer or hyperplasia and cells infected with viruses. These cells and tissues are not limited to those collected from patients that are subjects of treatment, and cells and tissues collected from other patients or other animals may also be used.

Cells and tissues infiltrated with lymphocytes are transplanted into highly immunodeficient animals in the same manner as in the aforementioned method for proliferating or producing plasma cells, and are recovered after proliferation of lymphocytes has been detected. Herein, the recovered transplanted cells in which lymphocytes have proliferated may be directly used as a therapeutic composition, or may be used as a therapeutic composition after having selected and separated the antibody-producing plasma cells, lymphocytes and the like by microdissection and such. Moreover, plasma cells and the like may be selected and separated from blood collected from highly immunodeficient animals transplanted with cells and the like infiltrated with lymphocytes, and used as a therapeutic composition.

The recovered transplanted cells or separated lymphocytes and the like can be further cultured and proliferated in vitro.

Moreover, instead of using lymphocytes such as plasma cells activated using highly immunodeficient animals, therapeutic compositions for lesion tissues arising as a result of cancer or viral infection may also be produced by using antibodies produced from plasma cells or antibody-encoding nucleic acids. The antibodies or antibody-encoding nucleic acids used herein can be those produced by the aforementioned methods of the present invention for producing antibodies and for producing nucleic acids encoding antibodies. When antibodies are used for therapeutic compositions, in addition to the antibodies' direct attack against abnormal substances such as cancer cells, virus-infected cells, and such, antibodies may also be used as a means of transporting anticancer agents and antiviral agents to cancer cells, virus-infected cells, and the like by binding anticancer agents or antiviral agents to the antibodies. Moreover, nucleic acids encoding antibodies may be similarly used; i.e. they may be administered to human patients either as is or with the support of an expression vector, and make the antibodies expressed in the body attack the abnormal substances in lesion tissues. Alternatively, the antibody-encoding nucleic acids of the present invention may also be fused with nucleic acids encoding another polypeptide having an anticancer or antiviral effect and used for transporting polypeptides having an anticancer or antiviral effect to abnormal cells.

All prior art references cited herein are incorporated by reference into this description.

EXAMPLES

Herein below, the present invention will be specifically described using Examples, but it is not to be construed as being limited thereto.

Example 1 Accumulation of Specific Plasma Cells and Increase of Antibody Titer in NOG Mice

Tumor tissues removed with consent from cancer patients during surgery were subcutaneously transplanted into NOG mice with the purpose of establishing cancer cell lines using NOG mice, Transplantation was carried out in the same manner using SCID mice as a control. Specifically, human breast cancer tissues were sliced into thin sections, and equal amounts were subcutaneously transplanted into NOG mice and SCID mice.

Transplantation was carried out with the supposition that transplantation efficiency would be higher in NOG mice as compared to nude mice, which have B cells and NK cells, and SCID mice, which have NK cells (Nature 301: 527-530, 1983); however, contrary to expectations, the transplantation efficiency was low (data not shown).

To find out the reasons for the above, cancer tissues were transplanted into NOG mice and SCID mice as described above and mice were dissected nine weeks later to recover the transplants. The transplants were embedded in OCT compound, and frozen blocks were prepared and stored in a deep freezer. A portion of the transplants were fixed in PFA, embedded in paraffin using the Amex method, sliced into thin sections, stained with HE, and pathological observations were carried out.

As a result, surprising findings were obtained. Namely, pathological images of a significantly high accumulation of plasma cells in the cancer tissues of NOG mice were observed during histopathological analyses, as compared to SCID mice, suggesting that the antibodies produced by the plasma cells may be attacking the cancer tissues (FIG. 1). A comparison with pathological images prior to transplantation confirmed that an even higher condensation of plasma cells was occurring in NOG mice (data not shown).

Cancer cells employ various strategies to escape from the host's immune system. The most common method is to reduce the expressed HLA antigen to prevent cancer antigens from being presented to immunocompetent cells (Moller et al, (1992) Cancer Surv 13:101). Moreover, TGF-β secreted by cancer cells has been reported to compete with IL-12 and prevents the activation of tumor immunity (Mouri (2002) Acta Med Okayama 56:309). In addition, the body's immune responses are suppressed by secretion of indoleamine 2,3-dioxygenase and Fas ligand (Zheng et al. (2003) Gast Cancer 9:1415; Reference 34/Uyttenhove et al. Nat Med 9: 1269). The present inventors conceived the possibility that lymphocyte activation occurs due to attenuation of the mechanism which suppresses the immune system in tumor tissues transplanted into highly immunodeficient non-human animals. Although tumor immunity comprises the cellular immune system mediated by cytotoxic T cells and NK cells, and the humoral immune system centered around antibodies, pathological observations revealed that the humoral immune system was particularly activated in transplanted tumor tissues.

Next, the titer of human-derived antibodies comprised in the serum of NOG mice was measured. Specifically, human breast cancer tissues were transplanted into NOG mice and the control SCID mice, blood was subsequently collected weekly from the orbital cavities of each mouse, sera were separated, and the antibody titers were monitored. As a result, IgG antibody titers in NOG mice showed values ten to a hundred times higher than in SCID mice. The highest values among NOG mice were confirmed to show an antibody titer of 10 mg/ml (FIG. 2).

The relationship between the degree of accumulation of plasma cells in transplants and the titer of human antibodies in the serum of NOG mice was investigated. The degree of accumulation of plasma cells was evaluated based on pathological observations and was classified according to the following criteria:

-   -   Grade 1: Small numbers of plasma cells are observed throughout         the tissue fragment.     -   Grade 2: Several accumulation foci of plasma cells are observed         throughout the tissue fragment.     -   Grade 3: Accumulation foci of plasma cells are observed across         multiple fields.

As was previously described, antibody titers were measured by collecting blood from the orbital cavities of mice, followed by separation of the serum. As a result, a high correlation was observed between the degree of accumulation of plasma cells in transplants and the antibody titer of human antibodies in the serum of NOG mice (FIG. 5).

Whether the high antibody titer in NOG mice was due to the effects of clearance in NOG mice was investigated. Human IgGs were administered to NOG mice and SCID mice to investigate their half-life. The half-life in NOG mice was about 18 days, while that in SCID mice was 21 days, with the half-life in NOG mice being slightly shorter (FIG. 6). Based on this finding, the high human antibody titers in NOG mice were shown not to be caused by a delay in clearance.

Example 2 Concentration and Separation of Plasma Cells in Breast Cancer Transplants and Amplification and Sequencing of the Antibody Genes

Fresh human breast cancer tissues were cut into suitable sizes and transplanted subcutaneously into NOG mice and SCID mice using a trocar. Following transplantation, blood was collected weekly from the orbital cavities of NOG mice, sera were separated, and the antibody titers were monitored. The antibody titers began to increase immediately after transplantation, reached a maximum value on week 5 following transplantation, and tended to decrease slowly thereafter (FIG. 4).

Mice (#1385, #1386, #1403, #1405) were dissected after the antibody titers were confirmed to have reached a maximum. Following dissection, the transplants were embedded in OCT compound, frozen blocks were prepared, and stored in a deep freezer. A portion of the transplants were fixed in PFA, embedded in paraffin using the Amex method, sliced into thin sections, stained with HE, and pathological observations were carried out. The frozen sections embedded in the OCT compound were thinly sliced and immediately subjected to RNA extraction, or sliced into thin sections and subjected to RNA extraction after excising plasma cells by LMD.

In the aforementioned procedures, total RNAs extracted directly from the thin sections and RNAs extracted after excising plasma cells by LMD were both purified using the RNeasy Mini Kit (QIAGEN). Based on these purified total RNAs, cDNAs were synthesized using Sensiscript Reverse Transcriptase (QIAGEN) according to the manufacturer's instructions. PCR amplifications were performed using these cDNAs as template and primers for cloning human antibody variable regions. Primers were designed based on the research paper “J. Mol. Biol. (1991) 222, 581-597”, and the web site of the Medical Research Council (MRC), “V BASE” (mrc-cpe.cam.ac.uk/vbase-ok.php?mene=901). Primer names starting with VH and JH correspond to primers for cloning heavy chain variable regions. Primer names starting with VK and JK, or VL and JL correspond to primers for amplifying the light chain κ chain or the light chain λ chain.

VH1a (SEQ ID NO: 1) 5′-CAGGT(GT)CAGCTGGTGCAGTCTGG-3′ VH1b (SEQ ID NO: 2) 5′-CAGGTCCAGCTTGTGCAGTCTGG-3′ VH1c (SEQ ID NO: 3) 5′-(GC)AGGTCCAGCTGGTACAGTCTGG-3′ VH1d (SEQ ID NO: 4) 5′-CA(AG)ATGCAGCTGGTGCAGTCTGG-3′ VH2a (SEQ ID NO: 5) 5′-CAGATCACCTTGAAGGAGTCTGGT-3′ VH2b (SEQ ID NO: 6) 5′-CAGGTCACCTTGA(AG)GGAGTCTGGT-3′ VH3a (SEQ ID NO: 7) 5′-GA(AG)GTGCAGCTGGTGGAGTCTGG-3′ VH3b (SEQ ID NO: 8) 5′-CAGGTGCAGCTGGTGGAGTCTGG-3′ VH3c (SEQ ID NO: 9) 5′-GAGGTGCAGCTGTTGGAGTCTGG-3′ VH4a (SEQ ID NO: 10) 5′-CAG(CG)TGCAGCTGCAGGAGTCGGGC-3′ VH4b (SEQ ID NO: 11) 5′-CAGGTGCAGCTACAGCAGTGGGGC-3′ VH5a (SEQ ID NO: 12) 5′-GA(AG)GTGCAGCTGGTGCAGTCTGGA-3′ VH6a (SEQ ID NO: 13) 5′-CAGGTACAGCTGCAGCAGTCAGGT-3′ VH7a (SEQ ID NO: 14) 5′-CAGGT(CG)CAGCTGGTGCAATCTGG-3′ JH1245 (SEQ ID NO: 15) 5′-TGAGGAGACGGTGACCAGGGT(GT)CC-3′ JH3 (SEQ ID NO: 16) 5′-TGAAGAGACGGTGACCATTGTCCC-3′ JH6 (SEQ ID NO: 17) 5′-TGAGGAGACGGTGACCGTGGTCCC-3′ VK1a (SEQ ID NO: 18) 5′-(AG)ACATCCAGATGACCCAGTCTCCA-3′ VK1b (SEQ ID NO: 19) 5′-G(AC)CATCCAGTTGACCCAGTCTCCA-3′ VK1c (SEQ ID NO: 20) 5′-GCCATCC(AG)GATGACCCAGTCTCCA-3′ VK1d (SEQ ID NO: 21) 5′-GTCATCTGGATGACCCAGTCTCCA-3′ VK2a (SEQ ID NO: 22) 5′-GATATTGTGATGACCCAGACTCCA-3′ VK2b (SEQ ID NO: 23) 5′-GAT(AG)TTGTGATGACTCAGTCTCCA-3′ VK3a (SEQ ID NO: 24) 5′-GAAATTGTGTTGAC(AG)CAGTCTCCA-3′ VK3b (SEQ ID NO: 25) 5′-GAAATAGTGATGACGCAGTCTCCA-3′ VK3c (SEQ ID NO: 26) 5′-GAAATTGTAATGACACAGTCTCCA-3′ VK4a (SEQ ID NO: 27) 5′-GACATCGTGATGACCCAGTCTCCA-3′ VK5a (SEQ ID NO: 28) 5′-GAAACGACACTCACGCAGTCTCCA-3′ VK6a (SEQ ID NO: 29) 5′-GAAATTGTGCTGACTCAGTCTCCA-3′ VK6b (SEQ ID NO: 30) 5′-GATGTTGTGATGACACAGTCTCCA-3′ JK1 (SEQ ID NO: 31) 5′-ACGTTTGATTTCCACCTTTGGTCCC-3′ JK24 (SEQ ID NO: 32) 5′-ACGTTTTGATCTCCA(CG)CTTGGTCCC-3′ JK3 (SEQ ID NO: 33) 5′-ACGTTTGATATCCACTTTGGTCCC-3′ JK5 (SEQ ID NO: 34) 5′-ACGTTTAATCTCCAGTCGTGTCCC-3′ VL1a (SEQ ID NO: 35) 5′-CAGTCTGTGCTGACTCAGCCACCC-3′ VL1b (SEQ ID NO: 36) 5′-CAGTCTGTG(CT)TGACGCAGCCGCCC-3′ VL2 (SEQ ID NO: 37) 5′-CAGTCTGCCCTGACTCAGCCT(CG)-3′ VL3a  (SEQ ID NO: 38) 5′-TCCTATG(AT)GCTGACTCAGCCACCC-3′ VL3b (SEQ ID NO: 39) 5′-TCCTATGAGCTGACACAGC(CT)ACCC-3′ VL3c (SEQ ID NO: 40) 5′-TCTTCTGAGCTGACTCAGGACCCT-3′ VL3d (SEQ ID NO: 41) 5′-TCCTATGAGCTGATGCAGCCACCC-3′ VL4a (SEQ ID NO: 42) 5′-CAGCCTGTGCTGACTCAATCATCC-3′ VL4b (SEQ ID NO: 43) 5′-CAGCTTGTGCTGACTCAATCGCCC-3′ VL4c (SEQ ID NO: 44) 5′-CTGCCTGTGCTGACTCAGCCCCCG-3′ VL5a (SEQ ID NO: 45) 5′-CAGCCTGTGCTGACTCAGCCA(CT)CT-3′ VL5c (SEQ ID NO: 46) 5′-CAGGCTGTGCTGACTCAGCCGGCT-3′ VL6 (SEQ ID NO: 47) 5′-AATTTTATGCTGACTCAGCCCCAC-3′ VL7 (SEQ ID NO: 48) 5′-CAG(AG)CTGTGGTGACTCAGGAGCCC-3′ VL8 (SEQ ID NO: 49) 5′-CAGACTGTGGTGACCCAGGAGCCA-3′ VL4_9 (SEQ ID NO: 50) 5′-C(AT)GCCTGTGCTGACTCAGCCACCT-3′ VL10 (SEQ ID NO: 51) 5′-CAGGCAGGGCTGACTCAGCCACCC-3′ JL1 (SEQ ID NO: 52) 5′-ACCTAGGACGGTGACCTTGGTCCC-3′ JL23 (SEQ ID NO: 53) 5′-ACCTAGGACGGTCAGCTTGGTCCC-3′ JL7 (SEQ ID NO: 54) 5′-ACCGAGGACGGTCAGCTGGGTGCC-3′ IgGrev (SEQ ID NO: 55) 5′-CGTCACCGGTTCGGGGAAGTAGTC-3′ IgMrev (SEQ ID NO: 56) 5′-GGGGAATTCTCACAGGAGACGAG-3′ IgKrev (SEQ ID NO: 57) 5′-GGCAGTTCCAGATTTCAACTGCT-3′

For cloning the heavy chain variable regions, κ chain variable regions, and λ chain variable regions, PCR amplifications were carried out using combinations of the Taq DNA polymerase Core Kit (QIAGEN) and primer mixtures for each gene subset. For amplifying the γ chain, μ chain, κ chain, and λ chain, five different primer mixtures were prepared for each. A total of 20 kinds of reaction solutions were prepared using these primer mixtures. Combinations of primers in the mixtures are shown in Table 1. Prepared reaction mixtures (20 μl) comprising 4 μl of the template cDNA had a final concentration of 1× reaction buffer, 1×Q solution (QIAGEN), 0.4 mM dNTP, 0.4 μM each of the forward and reverse primers, and 2 U Taq DNA polymerase. The reaction mixtures were subjected to 40 cycles of amplification reaction on Applied Biosystems PE9700. The amplification cycle was carried out under conditions of denaturation at 94° C. for 10 sec, annealing at 50° C. for 30 sec, and elongation at 72° C. for 30 sec.

TABLE 1 PRIMER SETS FORWARD REVERSE VH1-IgGrev MIX VH1a VH1b VH1c VH1d IgGrev VH2-IgGrev MIX VH2a VH2b IgGrev VH3/5-IgGrev MIX VH3a VH3b VH3c VH3d IgGrev VH4-IgGrev MIX VH4a VH4b IgGrev VH6/7-IgGrev MIX VH6a VH7a IgGrev VH1-IgMrev MIX VH1a VH1b VH1c VH1d IgMrev VH2-IgMrev MIX VH2a VH2b IgMrev VH3/5-IgMrev MIX VH3a VH3b VH3c VH3d IgMrev VH4-IgMrev MIX VH4a VH4b IgMrev VH6/7-IgMrev MIX VH6a VH7a IgMrev VK1-IgKrev MIX VK1a VK1b VK1c VK1d IgKrev VK2-IgKrev MIX VK2a VK2b IgKrev VK3-IgKrev MIX VK3a VK3b VK3c IgKrev VK4/5-IgKrev MIX VK4a VK5a IgKrev VK6-Igrev MIX VK6a VK6b IgKrev VL1/2-JL MIX VL1a VL1b VL2 JL1 JL23 JL7 VL3-JL MIX VL3a VL3b VL3c VL3d JL1 JL23 JL7 VL4-JL MIX VL4a VL4b VL4c JL1 JL23 JL7 VL5/6-JL MIX VL5a VL5c VL6 JL1 JL23 JL7 VL7_10-JL MIX VL7 VL8 VL4_9 VL10 JL1 JL23 JL7

Nested PCR amplification reactions were further carried out on the amplification products of the heavy chain variable regions (γ chain and μ chain) and the κ chain variable region. The combinations of primers used are shown in Table 2.

TABLE 2 PRIMER SETS FORWARD REVERSE VH1-JH MIX VH1a VH1b VH1c VH1d JH1245 JH3 JH6 VH2-JH MIX VH2a VH2b JH1245 JH3 JH6 VH3/5-JH MIX VH3a VH3b VH3c VH3d JH1245 JH3 JH6 VH4-JH MIX VH4a VH4b JH1245 JH3 JH6 VH6/7-JH MIX VH6a VH7a JH1245 JH3 JH6 VK1-JK MIX VK1a VK1b VK1c VK1d JK1 JK24 JK3 JK5 VK2-JK MIX VK2a VK2b JK1 JK24 JK3 JK5 VK3-JK MIX VK3a VK3b VK3c JK1 JK24 JK3 JK5 VK4/5-JK MIX VK4a VK5a JK1 JK24 JK3 JK5 VK6-JK MIX VK6a VK6b JK1 JK24 JK3 JK5

Example 3 Concentration and Separation of Plasma Cells in Prostate Cancer Transplants, Amplification and Sequencing of the Antibody Genes, and Production of ScFv

Based on the method indicated in Example 2, the variable regions of antibody genes produced by plasma cells, whose proliferation and accumulation were observed when prostate cancer or prostatic hyperplasia tissues were transplanted, were amplified by PCR. The primers and conditions used for PCR are the same as in Example 2.

A DNA fragment of antibody heavy chain variable region amplified by PCR was inserted into a pGEM-T Easy vector (Promega), and this was used to transform Escherichia coli DH5α. The nucleotide sequences of the insert sequence of the resulting transformed plasmids were determined. The determined nucleotide sequences are shown in SEQ ID NO: 58, 60, 62, 64, and 66. The translated amino acid sequences of these nucleotide sequences are respectively shown in SEQ ID NO: 59, 61, 63, 65, and 67. Among the 16 analyzed clones, eight sequences had a functional open reading frame, and of these, there were five independent sequences. Of the 16 clones, the sequences shown in SEQ ID NO: 64 and SEQ ID NO: 66 were found at a frequency of three and two times, respectively. The low level of sequence variety suggests that some form of selection pressure occurred causing clonal proliferation of plasma cells producing specific antibodies.

The linker sequences to be used for preparing single-stranded antibody genes were produced according to the method of Marks et al. (J. Mol. Biol. (1991) 222, 581-597). The template DNA sequences and the nucleotide sequences of primers used are shown below. Linker fragments synthesized using PCR amplification were confirmed by agarose gel electrophoresis, then excised and purified.

Template DNA Sequence (Template Linker)

(SEQ ID NO: 68) 5′-GGACAATGGTCACCGTCTCTTCAGGTGGTGGTGGTTCGGGTGGTGGT GGTTCGGGTGGTGGCGGATCGGACATCCAGATGACCCAGTCTCC-3′ Nucleotide Sequences of Primers: Reverse JH for Linker

1 LJH1_2 (SEQ ID NO: 69) 5′-GCACCCTGGTCACCGTCTCCTCAGGTGG-3′ 2 LJH3 (SEQ ID NO: 70) 5′-GGACAATGGTCACCGTCTCTTCAGGTGG-3′ 3 LJH4_5 (SEQ ID NO: 71) 5′-GAACCCTGGTCACCGTCTCCTCAGGTGG-3′ 4 LJH6 (SEQ ID NO: 72) 5′-GGACCACGGTCACCGTCTCCTCAGGTGG-3′ Reverse VK for Linker

5 LVK1 (SEQ ID NO: 73) 5′-GGAGACTGGGTCATCTGGATGTCCGATCCGCC-3′ 6 LVK2 (SEQ ID NO: 74) 5′-GGAGACTGAGTCATCACAACATCCGATCCGCC-3′ 7 LVK3   (SEQ ID NO: 75) 5′-GGAGACTGCGTCAACACAATTTCCGATCCGCC-3′ 8 LVK4 (SEQ ID NO: 76) 5′-GGAGACTGGGTCATCACGATGTCCGATCCGCC-3′ 9 LVK5 (SEQ ID NO: 77) 5′-GGAGACTGCGTGAGTGTCGTTTCCGATCCGCC-3′ 10 LVK6 (SEQ ID NO: 78) 5′-GGAGACTGAGTCAGCACAATTTCCGATCCGCC-3′ Reverse VL for Linker

11 LVL1 (SEQ ID NO: 79) 5′-GGCGGCTGCGTCAACACAGACTGCGATCCGCCACCGCCAGAG-3′ 12 LVL2 (SEQ ID NO: 80) 5′-GCAGGCTGAGTCAGAGCAGACTGCGATCCGCCACCGCCAGAG-3′ 13 LVL3a (SEQ ID NO: 81) 5′-GGTGGCTGAGTCAGCACATAGGACGATCCGCCACCGCCAGAG-3′ 14 LVL3b (SEQ ID NO: 82) 5′-GGGTCCTGAGTCAGCTCAGAAGACGATCCGCCACCGCCAGAG-3′ 15 LVL4 (SEQ ID NO: 83) 5′-GGCGGTTGAGTCAGTATAACGTGCGATCCGCCACCGCCAGAG-3′ 16 LVL5 (SEQ ID NO: 84) 5′-GACGGCTGAGTCAGCACAGACTGCGATCCGCCACCGCCAGAG-3′ 17 LVL6 (SEQ ID NO: 85) 5′-TGGGGCTGAGTCAGCATAAAATTCGATCCGCCACCGCCAGAG-3′

The heavy chain variable region, κ chain variable region, or λ chain variable region and linker sequence amplified by PCR were mixed, and PCR was carried out using the primer sets indicated below, A VH primer and JK primer combination was used to prepare reaction solutions when the light chain was a κ chain, while a VH primer and JL primer combination was used to prepare reaction solutions when the light chain was a λ chain. The reaction solutions were prepared using Ex Taq DNA polymerase (TaKaRa) according to instructions from the manufacturer. Denaturation at 94° C. for 1 minute, then 30 cycles of denaturation at 94° C. for 15 seconds and an elongation reaction at 68° C. for 1 minute were carried out to assemble and amplify a single strand antibody gene library.

VH1BACKSfi (SEQ ID NO: 86) 5′-GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCCAGGTGCAGCTGGTGCAGTCTGG-3′ VH2BACKSfi (SEQ ID NO: 87) 5′-GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCCAGGTCAACTTAAGGGAGTCTGG-3′ VH3BACKSfi (SEQ ID NO: 88) 5′-GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCGAGGTGCAGCTGGTGGAGTCTGG-3′ VH4BACKSfi (SEQ ID NO: 89) 5′-GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCCAGGTGCAGCTGCAGGAGTCGGG-3′ VH5BACKSfi (SEQ ID NO: 90) 5′-GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCCAGGTGCAGCTGTTGCAGTCTGC-3′ VH6BACKSfi (SEQ ID NO: 91) 5′-GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCCAGGTACAGCTGCAGCAGTCAGG-3′ JK1FORNot (SEQ ID NO: 92) 5′-GAGTCATTCTCGACTTGCGGCCGCACGTTTGATTTCCACCTTGGTCCC-3′ JK2FORNot (SEQ ID NO: 93) 5′-GAGTCATTCTCGACTTGCGGCCGCACGTTTGATCTCCAGCTTGGTCCC-3′ JK3FORNot (SEQ ID NO: 94) 5′-GAGTCATTCTCGACTTGCGGCCGCACGTTTGATATCCACTTTGGTCCC-3′ JK4FORNot (SEQ ID NO: 95) 5′-GAGTCATTCTCGACTTGCGGCCGCACGTTTGATCTCCACCTTGGTCCC-3′ JK5FORNot (SEQ ID NO: 96) 5′-GAGTCATTCTCGACTTGCGGCCGCACGTTTAATCTCCAGTCGTGTCCC-3′ JL1FORNot (SEQ ID NO: 97) 5′-GAGTCATTCTCGACTTGCGGCCGCACCTAGGACGGTGACCTTGGTCCC-3′ JL2_3FORNot (SEQ ID NO: 98) 5′-GAGTCATTCTCGACTTGCGGCCGCACCTAGGACGGTCAGCTTGGTCCC-3′ JL4_5FORNot (SEQ ID NO: 99) 5′-GAGTCATTCTCGACTTGCGGCCGCACCTAAAACGGTGAGCTGGGTCCC-3′

After confirming the amplification products by agarose gel electrophoresis, the bands comprising the corresponding gene fragments were excised and purified. The excised fragments were cleaved with the restriction enzymes StiI and NotI and inserted into the phagemid vector pCANTAB5E (Amersham Bioscience). The scFv protein encoded by the fragment inserted into the phagemid is expressed as a fusion protein with the M13 phage gene III and presented on M13 phages during infection with helper phages. Escherichia coli TG1 were transformed with the scFv library phagemids, and the inserted nucleotide sequences of clones randomly selected from the resulting E. coli library were clarified. The nucleotide sequences of the scFv single chain antibodies determined in the present Example are shown in SEQ ID NO: 100, 102, 104, 106, 108, and 110, while the translated amino acid sequences are shown in SEQ ID NO: 101, 103, 105, 107, 109, and 111.

The scFv E. coli library having random combinations of heavy chain variable regions and light chain variable regions was infected with the helper phage M13K07 to produce a phage library presenting scFv proteins on the phages. 0.2 ml of phage precipitation solution (20% polyethylene glycol (average molecular weight: 8000), 2.5 M NaCl) was added to 1 ml of phage solution, mixed well, and incubated on ice for 30 minutes. Phages were subsequently precipitated by centrifugation. This precipitate was suspended in a 2% skim milk-PBS solution and a blocking reaction was carried out at room temperature for one hour.

The phage clones were concentrated and selected using the binding activity toward the cell surface of the DU145 prostate cancer line cells as an index. DU145 cells were cultured at 37° C. and under 5% CO₂ in RPMI1640 medium containing 10% fetal bovine serum (FBS). After washing the proliferating adherent DU145 cells with PBS, cells were removed from the dishes using PBS containing 1 mM EDTA. After centrifuging the cell suspension once, the cells were resuspended in 2% FBS/PBS to 2×10⁶ cells/ml. An equal volume of scFv phage library solution was added to the cell suspension and this was incubated for 2 hours while shaking at 4° C. The mixture was centrifuged with the purpose of separating phages that bound to the cells from those that did not bind, precipitated cells were collected and resuspended in 2% FBS/PBS. After repeating this washing procedure for a total of five times, E. coli TG1 in a logarithmic growth phase were added to the precipitated cells, and phages that bound to the cells were collected. Cloning was carried out by adding TG1 and incubating at 37° C. for 1 hour, then plating the TG1 solution onto a medium containing the drug marker ampicillin, and incubating overnight at 37° C. to let colonies form.

Concentration and selection of phage clones were carried six times in total using the binding activity towards the cell surface as an index. DU145 cells were stained using a solution of scFv-presenting phage library selected by the binding to viable cell surfaces, and then subjected to a flow cytometry analysis. Specifically, immunostaining was carried out by mixing DU145 cells and the phage library solution, reacting a mouse anti-M13 antibody against M13 phage coat proteins (Amersham Bioscience) as a secondary antibody followed by reacting a FITC-labeled goat anti-mouse IgG antibody (Becton-Dickinson) as a tertiary antibody. The staining of the cells was analyzed by FACS Calibur (Becton-Dickinson) (FIG. 9). As the rounds of concentration and selection were carried out four to five times, the amount of phage that bound to the cells increased. Bound phages were cloned from libraries in which the proportion of cell-bound phages had increased, and from these libraries, bound clones 5-16 and 6-24 were identified after five and six rounds of concentration and selection, respectively (FIG. 10). The nucleotide sequences of the identified clones are shown in SEQ ID NO: 112 and 114, while the translated amino acid sequences are shown in SEQ ID NO: 113 and 115.

A vector that expresses and secretes a chimeric protein in an animal cell system was constructed. This chimeric protein has an amino acid sequence corresponding to SEQ ID NO: 113 fused to a constant region sequence on the C-terminal side of mouse IgG2a hinge region. The expression cassette was designed so that a secretion signal sequence derived from a human heavy chain immunoglobulin is added to the N-terminus. The nucleotide sequence encoding this scFv fusion protein is shown in SEQ ID NO: 116, while the translated sequence is shown in SEQ ID NO: 117. The expression vector (comprising a G418 drug resistance gene) was introduced into CHO cells by electroporation, and stably expressing cell lines were selected by the sandwich ELISA method. Coating was performed under weakly alkaline conditions after diluting a goat anti-mouse IgG (gamma) antibody (Zymed, 62-6600) 1000 folds. After washing, blocking was carried out with a blocking solution containing BSA. After adding the culture supernatant and capturing the scFv fusion proteins, the captured amount was detected with an alkaline phosphatase-labeled rabbit anti-mouse IgG2a antibody. Stable cell lines with a high protein expression level were cultured and scFv fusion proteins were prepared by purification from the culture supernatant using HiTrap Protein A (Amersham Bioscience). Analysis of the purified scFv fusion proteins was confirmed by SDS-PAGE and silver staining (FIG. 11). The purified scFv fusion proteins were confirmed to bind to DU145 by flow cytometry (FIG. 12).

Example 4 Flow Cytometry Analysis Using NOG Serum

Prostate cancer and benign prostatic hyperplasia specimens were transplanted into NOG mice. Following transplantation, blood was regularly collected from the orbital cavity of mice, the serum was separated, and changes in the titer of human antibodies (IgG IgM) were monitored. An increase in antibody titer was observed in six mice transplanted with four of the approximately 40 specimens (FIG. 3). These antibodies were diluted to 50 μg/ml and reacted with prostate cancer cell lines (DU145, PC3, LNCaP, and 22Rv1). After reacting for a predetermined amount of time, FITC-labeled anti-human IgG or IgM antibodies were added and the reaction was allowed to proceed again. After the reaction, whether or not cells were stained was confirmed by flow cytometry. As a result, human IgG antibodies of NOG mouse #1321, which was transplanted with the benign prostatic hyperplasia specimen, was shown to have recognized surface antigens of the prostate cancer cell line DU145 (FIG. 7).

Changes in human antibody titers in NOG mice transplanted with breast cancer specimens were similarly monitored. An increase in human antibody titer was observed in five mice transplanted with four of the ten specimens (FIG. 4). Cancer cell lines (MCF-7, MDA-MB-231, ZR-75-1, and BT-474) were immunostained in the same way as above using these antibodies and analyzed by flow cytometry. As a result, antibodies recognizing the cancer cell line ZR-75-1 were present among the human IgM antibodies in the sera of NOG mice #1385, #1386, and #1403 transplanted with breast cancer (FIG. 8).

Example 5 Detection by Flow Cytometry and Immunohistological Staining of Antitumor Antibodies Present in the Serum of NOG Mice Transplanted with Human Stomach Cancer

Cancer tissues excised from twelve stomach cancer patients were transplanted into NOG mice, and the titer of human antibodies (IgG, IgM) was monitored in the same manner as with prostate cancer. NOG sera in which the human antibody titer reached 50 μg/ml or more were analyzed by flow cytometry using four types of stomach cancer lines (AGS, KATO III, SNU-1, and SNU-5) to see whether they comprised antibodies recognizing cancer cell lines. IgGs and IgMs in the sera of mice transplanted with PLR0530 reacted strongly with the human cancer cell line AGS (the details of which are described in Example 6), and the IgMs in the sera of mice transplanted with PLR0631 and PLR0659 similarly showed a strong reaction with AGS. Moreover, IgMs in the sera of mice transplanted with PLR0624 reacted strongly with SNU-1. Sera of mice transplanted with PLR0624 and PLR0631 were further diluted, the IgM concentration was adjusted to 10 μg/ml, 2 μg/ml, or 0.4 μg/ml, and an analysis by flow cytometry was carried out. Results are shown in FIGS. 13 a and 13 b.

Next, using cell lines established at PharmaLogicals Research Pte Ltd, antibodies comprised in the sera of NOG mice were investigated by immunohistological staining to see whether those that recognize the cytoplasmic membrane of cancer cells are present. Immunohistological staining was carried out with a tissue array produced with an established cell line; the method of production is as follows: cancer cell lines serially engrafted for three or more generations in NOG mice were removed, fixed overnight with 4% paraformaldehyde, washed for two hours with 0.01 M phosphate buffer, and embedded in paraffin according to the AMeX method (Reference: Sato Y et al. (1986) Am J. Pathol. 125(3): 431-5). Cancer tissues with a diameter of 1.5 mm were excised from this block, transplanted into a new block of about 2.5 cm×3.0 cm, and a total of 36 different types (6×6) of cancer tissues were sequenced. The breakdown of the tissues is: 21 types of colorectal cancer; 4 types of small intestine cancer; 4 types of stomach cancer; and 1 type each of: adenocarcinoma of the ampulla of vater; breast cancer; bladder cancer; brain tumor; uterine cancer; lung cancer; and ovarian cancer. This tissue array was sliced into thin sections and after removing the paraffin, an immunohistological staining was carried out using the Ventana HX Discovery System (Ventana Medical Systems, Inc., Arizona, USA). Specifically, sera of NOG mice were diluted to an antibody concentration of 1 μg/ml, 2 μg/ml, or 10 μg/ml, added to the thinly sliced tissues, and reacted as primary antibodies. Moreover, biotin-SP-conjugated goat anti-human IgG antibodies (Jackson ImmunoResearch Labs) were added as secondary antibodies for the IgGs or biotin-SP-conjugated goat anti-human IgM antibodies (Jackson ImmunoResearch Labs) were added as secondary antibodies for the IgMs. Then a coloring reaction was carried out using DAB. An IHC with human IgGs present in the sera of mice transplanted with eleven different stomach cancer specimens confirmed a reactivity toward membrane antigens of cancer cells for one specimen, while human IgMs in the sera of mice transplanted with seven different of stomach cancer specimens were confirmed to react with membrane antigens of cancer cells for five specimens. Of the positive clones, the results of PLR0659 and PLR0530 are shown in the tables below (Tables 3 and 4). As evidenced from the tables, IgM antibodies comprised in the sera of mice transplanted with PLR0659 not only bound to the membranes of all four types of stomach cancer cells, but binding to membrane antigens of multiple colorectal cancers and small intestine cancers was also confirmed. On the other hand, the IgGs did not recognize the membrane antigens of cancer cells, and only recognized nuclear antigens. Reactivity to nuclear antigens was also observed for IgMs in all cases. It is presumed that nuclear antigens were exposed from a portion of cancer cells that denatured or died by necrosis in the course of proliferation, and antinuclear antibodies were produced in the body. Typical examples in which a staining of membrane antigens was observed by immunohistological staining are shown in FIGS. 14 a and 14 b.

TABLE 3 NOG SERUM A^(b) B (PRIMARY ANTIBODY) LOCATION OF 1 2 3 4 5 6 1 2 3 PLR MOUSE SERUM POSITIVE COLON AND/OR RECTUM No. No. No. Ig REACTIONS 00023 00030 00059 00082 00087 00119 00122 00123 00151 00659 2092 1452 G CELL MEMBRANE − − − − − − − − − NUCLEUS + + + + + + + + + M LUMINAL SIDE − − + + − − − − − CELL MEMBRANE OUTER BASAL + + + + − − + + + CELL MEMBRANE CELL MEMBRANE − − − − − − − − − MUCOSAL − − − − − − − + − SUBSTANCE NUCLEUS + + + + + + + + + NOG SERUM B C (PRIMARY ANTIBODY) LOCATION OF 4 5 6 1 2 3 4 5 6 PLR MOUSE SERUM POSITIVE COLON AND/OR RECTUM No. No. No. Ig REACTIONS 00168 00215 00233 00241 00254 00261 00273 00325 00355 00659 2092 1452 G CELL MEMBRANE − − − − − − − − − NUCLEUS + + + + + + + + + M LUMINAL SIDE − − − − − − − − − CELL MEMBRANE OUTER BASAL + − − + − + − − − CELL MEMBRANE CELL MEMBRANE − + − − − − − − − MUCOSAL − − − − − − − − − SUBSTANCE NUCLEUS + + + + + + + + + D E NOG SERUM 4 5 6 1 (PRIMARY ANTIBODY) LOCATION OF 1 2 3 VATER/ SMALL PLR MOUSE SERUM POSITIVE COLON AND/OR RECTUM DUODENUM INTESTINE No. No. No. Ig REACTIONS 00357 00379 00423 00077 00186 00229 00304 00659 2092 1452 G CELL MEMBRANE − − − − − − − NUCLEUS + + + + + + + M LUMINAL SIDE − − + − − − − CELL MEMBRANE OUTER BASAL − − + − − − + CELL MEMBRANE CELL MEMBRANE − − − − + − − MUCOSAL − − + + − − − SUBSTANCE NUCLEUS + + + + + + + NOG SERUM E F (PRIMARY ANTIBODY) LOCATION OF 2 3 4 5 6 1 2 3 PLR MOUSE SERUM POSITIVE STOMACH VATER BREAST BLADDER BRAIN No. No. No. Ig REACTIONS 00020 00269 00336 00339 00266 00478 00387 00032 00659 2092 1452 G CELL MEMBRANE − − − − − − − − NUCLEUS + + + + + + + + M LUMINAL SIDE − − − − − − − − CELL MEMBRANE OUTER BASAL − + − − + − − − CELL MEMBRANE CELL MEMBRANE + − + + − + + − MUCOSAL − − − − − − − − SUBSTANCE NUCLEUS + + + + + + + + NOG SERUM F (PRIMARY ANTIBODY) LOCATION OF 4 5 6 PLR MOUSE SERUM POSITIVE UTERUS LUNG OVARY No. No. No. Ig REACTIONS 00018 00327 00337 00659 2092 1452 G CELL MEMBRANE − − − NUCLEUS + + + M LUMINAL SIDE − − − CELL MEMBRANE OUTER BASAL − − − CELL MEMBRANE CELL MEMBRANE + + − MUCOSAL − − − SUBSTANCE NUCLEUS + + +

TABLE 4 NOG SERUM A B (PRIMARY ANTIBODY) LOCATION OF 1 2 3 4 5 6 1 2 3 PLR MOUSE SERUM POSITIVE COLON AND/OR RECTUM No. No. No. Ig REACTIONS 00023 00030 00059 00082 00087 00119 00122 00123 00151 00530 1619 980 G CELL MEMBRANE − − − − − − − − − NUCLEUS + + + + + + + + + M LUMINAL SIDE − − − − − − − − − CELL MEMBRANE OUTER BASAL − − − − − − − − − CELL MEMBRANE CELL MEMBRANE + − − − − − − − − MUCOSAL − − − − − − − − − SUBSTANCE NUCLEUS + + + + + + + + + NOG SERUM B C (PRIMARY ANTIBODY) LOCATION OF 4 5 6 1 2 3 4 5 6 PLR MOUSE SERUM POSITIVE COLON AND/OR RECTUM No. No. No. Ig REACTIONS 00168 00215 00233 00241 00254 00261 00273 00325 00355 00530 1619 980 G CELL MEMBRANE − − − − − − − − − NUCLEUS + + + + + + + + + M LUMINAL SIDE − − − + − − − − − CELL MEMBRANE OUTER BASAL − − − − − − − − − CELL MEMBRANE CELL MEMBRANE − − − − − − − − − MUCOSAL − − − + − − − − − SUBSTANCE NUCLEUS + + + + + + + + + D E NOG SERUM 4 5 6 1 (PRIMARY ANTIBODY) LOCATION OF 1 2 3 VATER/ SMALL PLR MOUSE SERUM POSITIVE COLON AND/OR RECTUM DUODENUM INTESTINE No. No. No. Ig REACTIONS 00357 00379 00423 00077 00186 00229 00304 00530 1619 980 G CELL MEMBRANE − − − − − − − NUCLEUS + + + + + + + M LUMINAL SIDE − − − − − − − CELL MEMBRANE OUTER BASAL − − − − − − − CELL MEMBRANE CELL MEMBRANE − − − − − − − MUCOSAL − − − − − − − SUBSTANCE NUCLEUS + + + + + + + NOG SERUM E F (PRIMARY ANTIBODY) LOCATION OF 2 3 4 5 6 1 2 3 PLR MOUSE SERUM POSITIVE STOMACH VATER BREAST BLADDER BRAIN No. No. No. Ig REACTIONS 00020 00269 00336 00339 00266 00478 00387 00032 00530 1619 980 G CELL MEMBRANE − − − − − − − − NUCLEUS 30 + + + + + + + M LUMINAL SIDE − − − − − − − − CELL MEMBRANE OUTER BASAL − + − − − − − − CELL MEMBRANE CELL MEMBRANE − − − − − − − − MUCOSAL − − − − − − − − SUBSTANCE NUCLEUS + + + + + + + + NOG SERUM F (PRIMARY ANTIBODY) LOCATION OF 4 5 6 PLR MOUSE SERUM POSITIVE UTERUS LUNG OVARY No. No. No. Ig REACTIONS 00018 00327 00337 00530 1619 980 G CELL MEMBRANE − − − NUCLEUS + + + M LUMINAL SIDE − − − CELL MEMBRANE OUTER BASAL − − − CELL MEMBRANE CELL MEMBRANE − − − MUCOSAL − − − SUBSTANCE NUCLEUS + + +

Example 6 Reactivity of Chimeric Antibodies Selected by Phage Panning Towards Cancer Cells

Since human IgGs and IgMs in the sera of NOG mice transplanted with the stomach cancer tissue PLR0530 reacted strongly with the stomach cancer cell line AGS (FIGS. 15 a and 15 b), an scFv-presenting phage library was produced from the variable region genes of antibodies produced by plasma cells that proliferated when stomach cancer sues were transplanted, based on the methods indicated in Examples 2 and 3. Concentration and selection of phage clones that bind to the cell surface of the stomach cancer cell line AGS were carried out according to the method indicated in Example 3. Following the concentration procedure, binding phages were cloned from libraries where an increase in the amount of binding phages was observed, and clone 1-3 which corresponds to SEQ ID NO: 118 was isolated (FIG. 16). The translated amino acid sequence corresponding to clone 1-3 is shown in SEQ ID NO: 119. An expression vector for scFv-mouse IgG2a constant region fusion protein corresponding to this clone sequence was constructed and introduced into CHO cells to establish a stably expressing cell line. The nucleotide sequence encoding the scFv fusion protein is shown in SEQ ID NO: 120, while the translated sequence is shown in SEQ ID NO: 121. Binding of the scFv fusion proteins purified from the culture supernatant (FIG. 17) to AGS cells was confirmed by flow cytometry (FIG. 18).

Next, an immunohistological staining of cancer tissues was carried out using this chimeric antibody. Stomach, colon, and small intestine provided from cancer patients were used as specimens. Each tissue comprises adjacent non-tumor tissues in addition to the cancer tissue. As a result of immunohistological staining, the following were stained in the stomach: cytoplasm of cancer cells, the cytoplasm of hyperplastic gastric mucosal cells, and the cytoplasm of normal gastric mucosal cells and gastric gland cells (FIG. 19). Moreover, the luminal side cell membrane and cytoplasm of cancer cells or normal mucosal membrane epithelial cells were stained in the colon, and the luminal side cell membrane and cytoplasm of hyperplastic mucosal membrane epithelial cells were stained in the small intestine (FIG. 19). In this manner, it was revealed that antibodies reacting to cancer cells and cancer tissues are obtained by this method. To obtain antibodies with a high specificity, it would be necessary to repeat this method and obtain several candidate clones.

INDUSTRIAL APPLICABILITY

Using the present invention, plasma cells that are infiltrating lesion tissues such as cancer tissues can be differentiated into antibody-producing plasma cells, and they can be proliferated and condensed to a high concentration. As a result, cells producing antibodies that recognize cancer cells and lesion tissues can be easily separated and obtained without having to clone antibody-producing cells in vitro. Moreover, antibody genes can be easily separated from these cells. The present invention is highly significant in the diagnosis and treatment of diseases such as cancer since it provides a method for easily acquiring genes for human antibodies that recognize lesion tissues such as cancer.

Antibodies are administered to humans during diagnoses and treatments that utilize antibodies. For example, during the diagnosis of cancer using antibodies, antibody molecules labeled with traceable labels are administered and the presence of cancer is indicated by the location of the antibodies. Moreover, with respect to treatment, in addition to the direct effect of the antibodies, antibodies onto which anticancer agents are bound are administered to patients. A high degree of safety is expected with human antibodies when administered to humans, and since the species is the same, concentrations in blood are expected to be stably maintainable for a long period of time.

Using the present invention, genes of cancer-specific antibodies can be efficiently separated from numerous cancer tissues. Moreover, it is also possible that the mechanism which directs the immune system towards a dominantly humoral immunity may be clarified. Therefore, the present invention has the potential of being useful in the development of not only antibodies but also low molecular weight pharmaceuticals such as those for treating cancer, autoimmune disease, infectious disease, and allergic disease. 

1. A method of producing cells which produce an antibody or antigen-binding portion thereof, wherein the method comprises the steps of: (a) transplanting a lesion tissue comprising infiltrating lymphocytes into a highly immunodeficient non-human animal, wherein the animal is not a severe combined immunodeficient (SCID) mouse; (b) detecting the proliferation of plasma cells at the site of transplantation; and (c) recovering a sample of the lesion tissue from the site of transplantation, wherein the sample comprises plasma cells.
 2. The method of claim 1, further comprising the step of: (d) excising a plasma cell from the recovered sample of lesion tissue and fusing the plasma cell with a partner cell.
 3. The method of claim 1, wherein the transplanted lesion tissue comprises cancer cells, hyperplasia cells, or virus-infected cells.
 4. The method of claim 3, wherein the transplanted lesion tissue comprises cells of a solid cancer or a blood cancer.
 5. The method of claim 4, wherein the transplanted lesion tissue comprises cells of a solid cancer that is a prostate cancer, stomach cancer, breast cancer, lung cancer, liver cancer, colorectal cancer, or pancreatic cancer.
 6. The method of claim 3, wherein the transplanted lesion tissue comprises cells of benign prostatic hyperplasia.
 7. The method of claim 1, wherein the highly immunodeficient non-human animal lacks NK cells.
 8. The method of claim 1, wherein the highly immunodeficient non-human animal lacks T cells, B cells, and NK cells.
 9. The method of claim 1, wherein the lesion tissue is from a human subject.
 10. The method of claim 1, wherein the antibody is a human antibody.
 11. The method of claim 1, wherein step (b) comprises determining the level of human antibodies in the serum of the animal, wherein a higher level of human antibodies in the serum is indicative of a higher number of plasma cells at the site of transplantation.
 12. A method of producing an antibody or antigen-binding portion thereof, wherein the antibody or antigen-binding portion thereof is isolated from the antibody-producing cells produced according to claim
 1. 13. The method of claim 12, wherein the transplanted lesion tissue comprises cancer cells, hyperplasia cells, or virus-infected cells.
 14. The method of claim 13, wherein the transplanted lesion tissue comprises cells of a solid cancer or a blood cancer.
 15. The method of claim 14, wherein the transplanted lesion tissue comprises cells of a solid cancer that is a prostate cancer, stomach cancer, breast cancer, lung cancer, liver cancer, colorectal cancer or pancreatic cancer.
 16. The method of claim 13, wherein the transplanted lesion tissue comprises cells of a benign prostatic hyperplasia.
 17. The method of claim 13, wherein the antibody or an antigen-binding portion thereof is an IgG, an IgM, an Fab, an F(ab′)2, an Fv, or a single chain Fv.
 18. The method of claim 17, wherein the antibody is an IgG.
 19. The method of claim 17, wherein the antibody is an IgM.
 20. The method of claim 17, wherein the antibody or antigen-binding portion thereof is a single chain Fv.
 21. The method of claim 12, further comprising conjugating the antibody or antigen-binding portion to a molecule selected from the group consisting of polyethylene glycol, a radioisotope, a chemotherapeutic, a cytotoxic substance, and a labeling substance.
 22. The method of claim 3, wherein the solid cancer is a prostate cancer.
 23. The method of claim 3, wherein the solid cancer is a stomach cancer.
 24. The method of claim 3, wherein the solid cancer is a breast cancer.
 25. The method of claim 3, wherein the solid cancer is a lung cancer.
 26. The method of claim 3, wherein the solid cancer is a liver cancer.
 27. The method of claim 3, wherein the solid cancer is a colorectal cancer.
 28. The method of claim 3, wherein the solid cancer is a pancreatic cancer.
 29. The method of claim 15, wherein the solid cancer is a prostate cancer.
 30. The method of claim 15, wherein the solid cancer is a stomach cancer.
 31. The method of claim 15, wherein the solid cancer is a breast cancer.
 32. The method of claim 3, wherein the solid cancer is a lung cancer.
 33. The method of claim 15, wherein the solid cancer is a liver cancer.
 34. The method of claim 15, wherein the solid cancer is a colorectal cancer.
 35. The method of claim 15, wherein the solid cancer is a pancreatic cancer. 